| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13612 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:116728530-116730060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr9:116729051-116729062 | CCACACCCTGC | + | 6.62 | | Nr5a2 | MA0505.1 | chr9:116728603-116728618 | CCAGGCCTTGAACTC | - | 6.06 | | ZNF410 | MA0752.1 | chr9:116729935-116729952 | GGATATTATGGGGTGGA | - | 7.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I113964 | chr9 | 116726436 | 116730118 |
|
Enhancer Sequence | TGCAGAGGGA GAAATCGAGG CCTTGGAAAT ACGTGTGACT TGCTGAAGAT CGCAGAGCTA 60
GAAAACGGCA AAACCAGGCC TTGAACTCCG ATGTTCTAAC TCTAAACTCT GTTCTCTTAA 120
GCTTCGGTTC AAATTGAGAC TCAGGTCAGT TTGCACAGGG TACAGATGAG TTTGCTGTTT 180
AGGTTGAATC ATATGAAACT GCTGGTGTTA GAACATTTTG GCCTCAGCAC ATGGCAATGT 240
CAGAGGTTCA GCTTAATCCA CTTGGAAGGA ATGGCTGTGA TGTATTTGTA AGGACAGACC 300
ACACCGGCCT GGCGTGTATG GAACTCCACC CTGGGAGTTG GTGTTCCCAA CACAGTGGAC 360
TTTGGCTCTG TCGTCATGGT GTAGCTGGAC TCGGCCAGGC CCACACGCTG TGATTGCCAG 420
GTGCTGTGAT ACTGACACAT GTGTCTTGGA CATCTCCCAC TGAATCCATT GTCCATCCAT 480
ATTCCAATGA AGCAACTCTC ATCTGCCACC ATCTGAACAT CCCACACCCT GCCCAGGTAG 540
AACTCTCCTC TAGTTGCCCC AGTTTCCCAG CAGCACCACC TGAGTCTCTG CAAAAGTATT 600
TGACAATTCT TTGAATATTT TTAGCACTTT CTCTTTGTTT TATGAAAATG GGTGGAAAAC 660
AGAAATGCAT GCAGCTACCA GTAACACGAA GCTGAAGTAT CATTCACTCA ATAAAAGAGA 720
AACAAAGGTG GAGATTATTA GGCATGCTGA AAACAGAGAC TCTTATCCCA CACTCTGTCA 780
CGTGTTTGCT GCACTTGAGC TGGTCAACTC TGTGTGAAAT TGTGAAGGAA AAGGACAAAA 840
ATGACAACTT TAAAAGTGTG TGTGACAAGC TAAAAATACA CGCACAGAAT TAAGTCTGAA 900
AGGCGAGAGA TCCATTTGGG AGTTAACCAT TTTTTTAAGA TCTCTGGGGC AGAATTTCCA 960
CCCGTACCAC TTCTGCTGCT TATGATACAA ACATTCAAAC AAATTCAGCC TGTTTGCTTT 1020
GCATACAAGT TTTGAGGAAT GCAAGATGTT GGAAAGAGGC TGTAATTGAT CTGTTCTTTT 1080
GCTCCCAGTG AAATGATATG CAAACCATTT TCTGCTTTCT TGTTTCTTCT GTTGAAATAA 1140
TACATGGGCA GCTCATTAAT TTCTTCCTCC CCGACCTCAC ATTTCTCCCT CCCTATTCGT 1200
CCTTAACCTT GCCCTTTCCC TTGTGTGGGA AACAGGAGCT GTTTGATGTC ACCCCATTTC 1260
CCAATTGGCT CTCCTGAATG TCGGTGGGAA GTAAAATGCT CCAGAACTGA GGATGTTGGA 1320
CTTTGGAGTG ACCCAGACCT GAGCTTATAG CTGTGGGACT TTTGATAAAT ACATTCTTTG 1380
ACCTGTGTTC TTGCCTGTAA AGTGGGGATA TTATGGGGTG GAGGGGGGAG GACCTATGGT 1440
GAGGATTAAA TGAGAGAAGG CATTAATGTC CACATCCTAG CGCCTAATGG GAAGTTCTCC 1500
CTGGGGAGCA AGTGTGGATG CCCGCTGGGA 1530
|
